Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
72 participants
OBSERVATIONAL
2017-10-25
2018-07-03
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Women with Psoriasis
Reproductive age women newly diagnosed with psoriasis
Hormone panel
Blood sampling on the 3rd day of menstrual cycle for the measurement of serum FSH,LH,PRL,E2 and AMH hormone levels.
Women without Psoriasis
Reproductive age women without psoriasis to serve as control
Hormone panel
Blood sampling on the 3rd day of menstrual cycle for the measurement of serum FSH,LH,PRL,E2 and AMH hormone levels.
Interventions
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Hormone panel
Blood sampling on the 3rd day of menstrual cycle for the measurement of serum FSH,LH,PRL,E2 and AMH hormone levels.
Eligibility Criteria
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Inclusion Criteria
* Women diagnosed with psoriasis (case group)
* Women without psoriasis (control group)
Exclusion Criteria
* history of ovarian surgery
* Body mass index (BMI) over 30
* Women with other autoimmune diseases including Hashitomo thyroiditis
* Women with family history of premature ovarian insufficiency (POI)
* Women with infertility
* Psoriasis using systemic drugs including steroids and immunosuppressive therapy.
18 Years
40 Years
FEMALE
Yes
Sponsors
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Kanuni Sultan Suleyman Training and Research Hospital
OTHER
Responsible Party
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Berna Aslan Cetin
Principle investigator
Principal Investigators
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Berna Aslan Cetin, MD
Role: PRINCIPAL_INVESTIGATOR
Kanuni Sultan Suleyman Research and Training Hospital
Locations
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Kanuni Sultan Suleyman Research and Training Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Related Links
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premature ovarian failure in patients with psoriasis
Other Identifiers
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2017/325
Identifier Type: -
Identifier Source: org_study_id
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